First examples of Friedel-Crafts alkylation using ketals as alkylating agents: an expeditious access to the benzene-fused8-oxabicyclo[3.2.1]octanering system.
Fan JF(范俊发) ; Wu YK(伍贻康) ; Wu YL(吴毓林)
刊名J. Chem. Soc.-Perkin Trans. 1
1999
页码1189-1191
ISSN号0300-922X
其他题名以缩酮为烷化剂的付-克烷化反应的首例:合成苯并-8-氧双环[3.2.1]辛烷环体系的简捷方法
通讯作者伍贻康
英文摘要A novel acid-catalyzed intramolecular Friedel -Crafts alkylation(cyclization) using a spiroketal as electrophile leading to the otherwise not easily accessible benzene-fused 8-oxabicyclo[3.2.1]octane ring system in synthetically useful yields is reported. Slightly more than one equivalent of BF+3.Oet=2 in THF at refluxing temperature are found to be the most satisfactory conditions to achieve the desiredcyclization. An electro-donating group para to the position where cyclization will take placegreatly facilitates the reactiion.
学科主题有机化学
收录类别SCI
原文出处http://dx.doi.org/10.1039/a900692c
语种英语
公开日期2013-01-17
内容类型期刊论文
源URL[http://202.127.28.38/handle/331003/13954]  
专题上海有机化学研究所_生命有机化学国家重点实验室
推荐引用方式
GB/T 7714
Fan JF,Wu YK,Wu YL. First examples of Friedel-Crafts alkylation using ketals as alkylating agents: an expeditious access to the benzene-fused8-oxabicyclo[3.2.1]octanering system.[J]. J. Chem. Soc.-Perkin Trans. 1,1999:1189-1191.
APA 范俊发,伍贻康,&吴毓林.(1999).First examples of Friedel-Crafts alkylation using ketals as alkylating agents: an expeditious access to the benzene-fused8-oxabicyclo[3.2.1]octanering system..J. Chem. Soc.-Perkin Trans. 1,1189-1191.
MLA 范俊发,et al."First examples of Friedel-Crafts alkylation using ketals as alkylating agents: an expeditious access to the benzene-fused8-oxabicyclo[3.2.1]octanering system.".J. Chem. Soc.-Perkin Trans. 1 (1999):1189-1191.
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